Cited 0 time in
Surface modification of LiNi0.5Mn1.5O4 cathodes with ZnAl2O4 by a sol-gel method for lithium ion batteries
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Lee, Yongho | - |
| dc.contributor.author | Mun, Junyoung | - |
| dc.contributor.author | Kim, Dong-Won | - |
| dc.contributor.author | Lee, Joong Kee | - |
| dc.contributor.author | Choi, Wonchang | - |
| dc.date.accessioned | 2022-07-16T06:25:35Z | - |
| dc.date.available | 2022-07-16T06:25:35Z | - |
| dc.date.issued | 2014-01 | - |
| dc.identifier.issn | 0013-4686 | - |
| dc.identifier.issn | 1873-3859 | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/160895 | - |
| dc.description.abstract | The 5 V spinel LiNi0.5Mn1.5O4 cathodes have been surface-modified with ZnAl2O4 by a sal-gel method and characterized by X-ray diffraction, high-resolution transmission electron microscopy, and electrochemical measurements. Although the pristine electrode experienced the prominent degradation after the storage test at 60 degrees C in the intervals of cycling test at room temperature, the ZnAl2O4-coated LiNi0.5Mn1.5O4 cathode exhibited the significant capacity retention even after storing at elevated temperatures. The X-ray photoelectron spectroscopy data reveals that the improved electrochemical performances of surface-coated cathode are mostly due to the suppressed side reaction between the cathode and the electrolyte especially at the high-temperature environment. Differential scanning calorimetry showed that the decreased heat evolution could be found with the surface-modified cathode. Our experimental findings suggest a direction to the further development of cathode materials which are endurable to the highly oxidized state and high-temperature environment. | - |
| dc.format.extent | 6 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | Pergamon Press Ltd. | - |
| dc.title | Surface modification of LiNi0.5Mn1.5O4 cathodes with ZnAl2O4 by a sol-gel method for lithium ion batteries | - |
| dc.type | Article | - |
| dc.publisher.location | 영국 | - |
| dc.identifier.doi | 10.1016/j.electacta.2013.10.127 | - |
| dc.identifier.scopusid | 2-s2.0-84888124344 | - |
| dc.identifier.wosid | 000331424300043 | - |
| dc.identifier.bibliographicCitation | Electrochimica Acta, v.115, pp 326 - 331 | - |
| dc.citation.title | Electrochimica Acta | - |
| dc.citation.volume | 115 | - |
| dc.citation.startPage | 326 | - |
| dc.citation.endPage | 331 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | sci | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Electrochemistry | - |
| dc.relation.journalWebOfScienceCategory | Electrochemistry | - |
| dc.subject.keywordPlus | ELECTROCHEMICAL PERFORMANCE | - |
| dc.subject.keywordPlus | HYDROTHERMAL SYNTHESIS | - |
| dc.subject.keywordPlus | ELECTRODE MATERIALS | - |
| dc.subject.keywordPlus | RATE CAPABILITY | - |
| dc.subject.keywordPlus | HIGH-POWER | - |
| dc.subject.keywordPlus | SPINEL | - |
| dc.subject.keywordPlus | LI | - |
| dc.subject.keywordPlus | LIMN1.5NI0.5O4 | - |
| dc.subject.keywordPlus | CO | - |
| dc.subject.keywordPlus | PARTICLES | - |
| dc.subject.keywordAuthor | Lithium ion battery | - |
| dc.subject.keywordAuthor | Lithium nickel manganese oxide | - |
| dc.subject.keywordAuthor | Surface modification | - |
| dc.subject.keywordAuthor | Zinc aluminate coating | - |
| dc.identifier.url | https://www.sciencedirect.com/science/article/pii/S0013468613020975?via%3Dihub | - |
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.
222, Wangsimni-ro, Seongdong-gu, Seoul, 04763, Korea+82-2-2220-1366
COPYRIGHT © 2024 HANYANG UNIVERSITY.
Certain data included herein are derived from the © Web of Science of Clarivate Analytics. All rights reserved.
You may not copy or re-distribute this material in whole or in part without the prior written consent of Clarivate Analytics.
